FDA NDC Directory · JSON-LD · Markdown

CIBINQO

NDC 63539-336 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameabrocitinib
Labeler / ManufacturerU.S. Pharmaceuticals
Marketing categoryNew Drug Application (innovator) · App NDA213871
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABROCITINIB (100 mg/1)
Marketing started20220224
Package count1

External sources

Source: openFDA. Public-domain (CC0).